Canonical Allele Identifier: CA497474038

Gene: PAFAH1B1

Linked Data

• MyVariant Identifiers: chr17:g.2577438T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.2674144T>C , CM000679.2:g.2674144T>C	GRCh38
NC_000017.10:g.2577438T>C , CM000679.1:g.2577438T>C	GRCh37
NC_000017.9:g.2524188T>C	NCBI36
NG_009799.1:g.85516T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000397195.10:c.756T>C MANE Select	ENSP00000380378.4:p.Cys252=
ENST00000571495.2:n.1841T>C
ENST00000674608.1:c.810T>C	ENSP00000501976.1:p.Cys270=
ENST00000674717.1:c.561T>C	ENSP00000501931.1:p.Cys187=
ENST00000675202.1:c.756T>C	ENSP00000502843.1:p.Cys252=
ENST00000675331.1:c.756T>C	ENSP00000502031.1:p.Cys252=
ENST00000675390.1:c.756T>C	ENSP00000501969.1:p.Cys252=
ENST00000675574.1:n.1828T>C
ENST00000675621.1:c.756T>C	ENSP00000502117.1:p.Cys252=
ENST00000675764.1:c.*710T>C	ENSP00000502242.1:n.*710T>C
ENST00000676077.1:c.*74T>C	ENSP00000502507.1:n.*74T>C
ENST00000676098.1:c.756T>C	ENSP00000502735.1:p.Cys252=
ENST00000676188.1:c.756T>C	ENSP00000502577.1:p.Cys252=
ENST00000676353.1:c.561T>C	ENSP00000502737.1:p.Cys187=
ENST00000397193.7:n.564T>C
ENST00000397195.9:c.756T>C	ENSP00000380378.4:p.Cys252=
ENST00000571495.1:n.480T>C
ENST00000572915.6:n.676+48T>C
ENST00000574468.1:c.252T>C	ENSP00000460591.1:p.Cys84=
ENST00000574816.5:n.31-2170T>C
NM_000430.3:c.756T>C	NP_000421.1:p.Cys252=
XM_011523901.1:c.810T>C	XP_011522203.1:p.Cys270=
XM_011523902.1:c.810T>C	XP_011522204.1:p.Cys270=
XM_011523903.1:c.810T>C	XP_011522205.1:p.Cys270=
XM_011523904.1:c.*74T>C	XP_011522206.1:n.*74T>C
XM_011523901.2:c.810T>C	XP_011522203.1:p.Cys270=
XM_011523902.3:c.810T>C	XP_011522204.1:p.Cys270=
XM_011523903.2:c.810T>C	XP_011522205.1:p.Cys270=
XM_017024701.1:c.756T>C	XP_016880190.1:p.Cys252=
XM_017024702.2:c.561T>C	XP_016880191.1:p.Cys187=
NM_000430.4:c.756T>C MANE Select	NP_000421.1:p.Cys252=